Interesting facts
Interesting Facts about 2-Methylnaphthalene-1,4-dione
2-Methylnaphthalene-1,4-dione, also known as 1,4-Dimethylnaphthalene, is a fascinating organic compound that belongs to the naphthoquinone family. Here are some intriguing aspects about this compound:
- Structure and Isomerism: This compound exhibits a unique structure characterized by a fused polycyclic system. The positioning of the methyl group at the 2 position leads to different properties and reactivity compared to its isomers.
- Biological Relevance: Naphthoquinones, including 2-methylnaphthalene-1,4-dione, have been studied for their potential biological activities such as antibacterial and anticancer properties, making them of great interest in medicinal chemistry.
- Reactivity: The presence of the diketone functional groups makes this compound reactive, opening pathways for various chemical transformations, including oxidation and reduction reactions.
- Applications: Beyond its role in research, this compound is also useful as a dye precursor in various industrial processes, showcasing its versatility.
- Environmental Aspect: Compounds like 2-methylnaphthalene-1,4-dione can be found in some natural processes and are studied in the context of environmental pollution and remediation strategies.
Its unique properties and interesting chemistry make 2-methylnaphthalene-1,4-dione a significant compound in the realm of organic chemistry. The potential to explore its applications and effects propels ongoing research in both academic and industrial settings.
Synonyms
menadione
58-27-5
Vitamin K3
2-Methyl-1,4-naphthoquinone
2-methylnaphthalene-1,4-dione
Menaphthone
Kayquinone
2-Methylnaphthoquinone
Thyloquinone
Kappaxin
Kayklot
Klottone
Kolklot
Panosine
Kanone
2-Methyl-1,4-naphthalenedione
Menadion
Menaphthon
Kipca
Prokayvit
Aquakay
Aquinone
Hemodal
Kaergona
Mitenon
Mitenone
Karcon
Kareon
Kativ-G
Kaykot
Koaxin
Synkay
K-Thrombyl
K-Vitan
Kappaxan
Juva-K
Vitamin K 3
Menaquinone 0
2-Methyl-1,4-naphthochinon
Vitamin K2(0)
Vitamin K0
Memodol
Usaf ek-5185
3-Methyl-1,4-naphthoquinone
Menaphtone
2-Methyl-1,4-naftochinon
1,4-Naphthalenedione, 2-methyl-
2-methyl-1,4-dihydronaphthalene-1,4-dione
Menaphthene
Kaynone
1,4-Naphthoquinone, 2-methyl-
Menadione (Vitamin K3)
NSC 4170
MFCD00001681
CCRIS 6672
HSDB 3354
Menaquinone O
Methyl-1,4-naphthoquinone
NSC-4170
EINECS 200-372-6
UNII-723JX6CXY5
723JX6CXY5
DTXSID4021715
MNQ
1,4-naphthalenedione, 2-methyl
CHEBI:28869
AI3-14700
NSC4170
Menadione [USP:BAN]
CHEMBL590
2-Methyl-1,4-naphthalendione
MLS000069420
DTXCID801715
Menadionum
Menadione (Vitamin K3) 10 microg/mL in Acetonitrile
34524-96-4
Kappaxan (VAN)
VK3
CAS-58-27-5
Menadione semiquinone
NCGC00016258-02
Menadione (USP:BAN)
SMR000059102
MENADIONE (MART.)
MENADIONE [MART.]
MENADIONE (USP-RS)
MENADIONE [USP-RS]
MENADIONE (EP MONOGRAPH)
MENADIONE [EP MONOGRAPH]
MENADIONE (USP MONOGRAPH)
MENADIONE [USP MONOGRAPH]
2-Methyl-1,4-naftochinon [Czech]
Menadione (USP)
Kappaxin (TN)
2-Methyl-1,4-naphthochinon [German]
PHYTOMENADIONE IMPURITY A (EP IMPURITY)
PHYTOMENADIONE IMPURITY A [EP IMPURITY]
SR-01000712386
2-Methyl-1,4-naphthodione
Methyl-1,4-naphthalenedione
Mendione
1,4-Dihydro-2-methylnaphthalene-1,4-dione
Menadione Phenolic
2-methyl-1,4-naphthoquinone, 5
Menadione, 9
Menadione,(S)
Phytomenadione Imp. A (EP); Menadione; 2-methylnaphthalene-1,4-dione; Phytomenadione Impurity A
Menadione1528
Prestwick_313
Menadione, 98%
Menadione (Standard)
Menadione, crystalline
Spectrum_001228
SpecPlus_000191
MENADIONE [MI]
MENADIONE [HSDB]
Opera_ID_1802
Prestwick0_000459
Prestwick1_000459
Prestwick2_000459
Prestwick3_000459
Spectrum2_001194
Spectrum4_000722
Spectrum5_001764
MENADIONE [VANDF]
M0373
NCIMech_000105
cid_4055
MENADIONE [WHO-DD]
2-methyl-1,4-napthoquinone
SCHEMBL25970
BSPBio_000538
KBioGR_000984
KBioGR_002527
KBioSS_001708
KBioSS_002535
2-methyl-1,4 naphthoquinone
MLS001148443
BIDD:ER0556
DivK1c_000080
DivK1c_006287
SPECTRUM1502254
SPBio_001267
SPBio_002477
3-methyl-1,4-naphthalenedione
BPBio1_000592
MENADIONE [ORANGE BOOK]
2-Methyl-[1,4]-naphthoquinone
BDBM24778
HMS500D22
HY-B0332R
KBio1_000080
KBio1_001231
KBio2_001708
KBio2_002527
KBio2_004276
KBio2_005095
KBio2_006844
KBio2_007663
KBio3_003005
WLN: L66 BV EVJ C1
cMAP_000077
NINDS_000080
Bio1_000471
Bio1_000960
Bio1_001449
HMS1569K20
HMS1921P06
HMS2092F12
HMS2096K20
HMS2232A09
HMS2234J16
HMS3371M08
HMS3373A12
HMS3655P03
HMS3869N03
Pharmakon1600-01502254
BCP25699
HY-B0332
STR01143
Tox21_110334
Tox21_301367
BBL027351
CCG-35354
Menadione (K3), analytical standard
NSC758200
s1949
STL377874
AKOS004910447
AKOS025244105
Tox21_110334_1
DB00170
FM11258
FS-2556
NSC-758200
SB17255
IDI1_000080
QTL1_000056
USEPA/OPP Pesticide Code: 006319
NCGC00016258-01
NCGC00016258-03
NCGC00016258-04
NCGC00016258-06
NCGC00016258-07
NCGC00016258-08
NCGC00094978-01
NCGC00094978-02
NCGC00255225-01
2-Methyl-1,4-naphthoquinone;Vitamin K3
AC-34841
NCI60_003945
SMR000653532
SY018303
SBI-0051776.P002
Menadione, meets USP testing specifications
NS00010106
SW219798-1
C05377
D02335
EN300-125382
Q192471
1,4-Naphthalenedione, 2-methyl-, radical ion(1-)
SR-01000712386-2
SR-01000712386-5
SR-01000712386-6
VITAMIN K3; 2-METHYL-1,4-NAPHTHALENEDIONE
BRD-K78126613-001-16-0
BRD-K78126613-001-27-7
BRD-K78126613-001-28-5
BRD-K78126613-001-29-3
Vitamin K3; 2-Methyl-1,4-naphthoquinone; Menaphthone
Vitamin K3: 1,4-Dihydro-1,4-dioxo-2-methylnaphthalene
Z1255430959
Menadione, European Pharmacopoeia (EP) Reference Standard
03AAE1E9-B215-45AF-976C-91E61894A467
Menadione, United States Pharmacopeia (USP) Reference Standard
Menadione, Pharmaceutical Secondary Standard; Certified Reference Material
InChI=1/C11H8O2/c1-7-6-10(12)8-4-2-3-5-9(8)11(7)13/h2-6H,1H
2-Methyl-1,4-naphthoquinone; Vitamin K2(0); Vitamin K3; 2-Methyl-1,4-dihydronaphthalene-1,4-dione
200-372-6
Solubility of 2-methylnaphthalene-1,4-dione
2-methylnaphthalene-1,4-dione (C11H8O2) exhibits interesting solubility characteristics primarily influenced by its chemical structure. The compound is relatively non-polar due to the naphthalene ring system, which affects its interaction with solvents. Here are some key points regarding its solubility:
In summary, the solubility of 2-methylnaphthalene-1,4-dione can be attributed to its non-polar characteristics, making it more compatible with organic solvents while exhibiting minimal solubility in polar solvent systems like water. This behavior highlights the importance of understanding solvent interactions in the context of such complex organic compounds.